Kim Mi Ju, Kim Hyun Mi, Cha Hyun-Hwa, Seong Won Joon
Department of Obstetrics and Gynecology, Kyungpook National University Hospital, School of Medicine, Kyungpook National University, Daegu, Korea.
J Yeungnam Med Sci. 2023 Nov;40(Suppl):S9-S16. doi: 10.12701/jyms.2023.00150. Epub 2023 May 8.
The aim of this study was to analyze the single nucleotide polymorphisms (SNPs) of genes known to be involved in vitamin D metabolism in the placenta using the placental tissue of mothers diagnosed with gestational diabetes mellitus (GDM) to determine whether the SNPs and occurrence of GDM are related.
We enrolled 80 women of the same gestational age, 40 with and 40 without GDM. The placenta was obtained from each woman after delivery and SNP genotyping was performed on seven SNPs in the CYP27B1 (rs10877012), CYP24A1 (rs2248359, rs6013897, and rs2209314), and GC (rs2282679, rs16847024, and rs3733359) genes. Maternal serum 25-hydroxyvitamin D levels were measured during the first trimester of pregnancy and before delivery.
At the time of delivery, vitamin D levels were lower (21.05±12.05 mg/dL vs. 31.31±20.72 mg/dL, p=0.012) and the frequency of vitamin D deficiency was higher (60.7% vs. 32.5%, p=0.040) in the GDM group. In women with GDM, the G allele of rs10877012 was more common (86.3% vs. 65.0%, p=0.002). The rs10877012 GG genotype was more common in the GDM group (72.5% vs. 42.5%, p=0.007) and the rs10877012 TT genotype was more common in the control group (12.5% vs. 0%, p=0.007).
Mothers with GDM have lower serum concentrations of vitamin D before delivery than healthy controls and vitamin D deficiency is common. A polymorphism in CYP27B1 (rs10877012), is considered to be a cause of GDM pathogenesis.
本研究旨在利用被诊断为妊娠期糖尿病(GDM)的母亲的胎盘组织,分析已知参与胎盘维生素D代谢的基因的单核苷酸多态性(SNP),以确定SNP与GDM的发生是否相关。
我们招募了80名相同孕周的女性,其中40名患有GDM,40名未患GDM。每位女性在分娩后获取胎盘,并对CYP27B1(rs10877012)、CYP24A1(rs2248359、rs6013897和rs2209314)以及GC(rs2282679、rs16847024和rs3733359)基因中的7个SNP进行基因分型。在妊娠早期和分娩前测量母亲血清25-羟基维生素D水平。
分娩时,GDM组的维生素D水平较低(21.05±12.05mg/dL对31.31±20.72mg/dL,p=0.012),维生素D缺乏的频率较高(60.7%对32.5%,p=0.040)。在患有GDM的女性中,rs10877012的G等位基因更为常见(86.3%对65.0%,p=0.002)。rs10877012的GG基因型在GDM组中更为常见(72.5%对42.5%,p=0.007),而rs10877012的TT基因型在对照组中更为常见(12.5%对0%,p=0.007)。
患有GDM的母亲在分娩前血清维生素D浓度低于健康对照组,维生素D缺乏很常见。CYP27B1(rs10877012)中的一种多态性被认为是GDM发病机制的一个原因。